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Associate Pilot Plant

  • ... Posted on: Dec 02, 2024
  • ... BioPharma Consulting JAD Group
  • ... West Greenwich, Rhode Island
  • ... Salary: Not Available
  • ... Contract

Associate Pilot Plant   

Job Title :

Associate Pilot Plant

Job Type :

Contract

Job Location :

West Greenwich Rhode Island United States

Remote :

No

Jobcon Logo Job Description :

Job Description:

We are seeking a highly motivated and self-driven individual to support the execution of cell culture and downstream purification processes. The ideal candidate will have a strong work ethic, eagerness to learn, and the ability to work independently.

Responsibilities:

  • Support cell culture processes, including aseptic vial thawing, cell culture flask passaging in biosafety cabinets, and operation of benchtop wave bioreactors, as well as 200L and 500L single-use bioreactors.
  • Assist with large-scale harvest operations through downstream purification, including chromatography, filtration, and Ultra-Filtration/Diafiltration (UF/DF) using pilot-scale skids and equipment.
  • Perform routine tasks such as in-process sampling, operating laboratory analyzers, managing samples, and collecting scientific data via electronic laboratory notebooks.
  • Compound media/buffer solutions and perform Clean-In-Place (CIP) and Steam-In-Place (SIP) procedures.
  • Assemble and disassemble equipment, provide routine maintenance for benchtop analyzers, and support vendor oversight.
  • Maintain lab organization, cleanliness, and adherence to safety protocols.
  • Utilize scientific principles for experiment execution and data analysis in a collaborative team environment.
  • Document data and process information in accordance with Good Documentation Practices (GDP).
  • Contribute to maintaining laboratory standards with a focus on safety, quality, and compliance.

Requirements

Qualifications:

Basic Qualifications:

  • Bachelor’s Degree in Engineering or Science, or
  • Associate’s Degree with 1+ year of experience in a laboratory or manufacturing setting, or
  • 2+ years of experience in a laboratory or manufacturing setting.
  • Ability to work weekends.

Preferred Qualifications:

  • Prior hands-on experience in pilot- or large-scale cell culture or downstream purification process development or manufacturing.
  • Experience with automated computer-controlled biopharmaceutical equipment.
  • Knowledge of process data compilation and analysis.
  • Demonstrated problem-solving capabilities with excellent attention to detail.
  • Strong written and verbal communication skills.

Jobcon Logo Position Details

Posted:

Dec 02, 2024

Employment:

Contract

Salary:

Not Available

Snaprecruit ID:

SD-WOR-3038ff94a87d177502cfedbd0b36613a7c03783c4a6cd974fa9e065979a70a94

City:

West Greenwich

Job Origin:

WORKABLE_ORGANIC_FEED

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Job Description:

We are seeking a highly motivated and self-driven individual to support the execution of cell culture and downstream purification processes. The ideal candidate will have a strong work ethic, eagerness to learn, and the ability to work independently.

Responsibilities:

  • Support cell culture processes, including aseptic vial thawing, cell culture flask passaging in biosafety cabinets, and operation of benchtop wave bioreactors, as well as 200L and 500L single-use bioreactors.
  • Assist with large-scale harvest operations through downstream purification, including chromatography, filtration, and Ultra-Filtration/Diafiltration (UF/DF) using pilot-scale skids and equipment.
  • Perform routine tasks such as in-process sampling, operating laboratory analyzers, managing samples, and collecting scientific data via electronic laboratory notebooks.
  • Compound media/buffer solutions and perform Clean-In-Place (CIP) and Steam-In-Place (SIP) procedures.
  • Assemble and disassemble equipment, provide routine maintenance for benchtop analyzers, and support vendor oversight.
  • Maintain lab organization, cleanliness, and adherence to safety protocols.
  • Utilize scientific principles for experiment execution and data analysis in a collaborative team environment.
  • Document data and process information in accordance with Good Documentation Practices (GDP).
  • Contribute to maintaining laboratory standards with a focus on safety, quality, and compliance.

Requirements

Qualifications:

Basic Qualifications:

  • Bachelor’s Degree in Engineering or Science, or
  • Associate’s Degree with 1+ year of experience in a laboratory or manufacturing setting, or
  • 2+ years of experience in a laboratory or manufacturing setting.
  • Ability to work weekends.

Preferred Qualifications:

  • Prior hands-on experience in pilot- or large-scale cell culture or downstream purification process development or manufacturing.
  • Experience with automated computer-controlled biopharmaceutical equipment.
  • Knowledge of process data compilation and analysis.
  • Demonstrated problem-solving capabilities with excellent attention to detail.
  • Strong written and verbal communication skills.

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